Hydroxychloroquine Sulfate 68071-3955

Product NDC

68071-3955

Manufacturer: Nucare Pharmaceuticals, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 1, 2019
Listing Expires: December 31, 2027
Application: ANDA040657

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Active Ingredients

Ingredient	Strength
Hydroxychloroquine Sulfate	200 mg/1

Drug Class

Antimalarial [EPC]Antirheumatic Agent [EPC]

Packaging Options(1)

68071-3955-06

60 TABLET, FILM COATED in 1 BOTTLE (68071-3955-6)

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